| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55572283-55572561 | Common:1; Rare:107 | ||||
| chr7:55951730-55951930 | Rare:59 | ||||
| chr7:55964406-55964685 | Common:1; Rare:96 | ||||
| chr7:56051424-56051845 | Common:1; Rare:161; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:64794277-64794463 | Common:4; Rare:51 | ||||
| chr7:64903119-64903277 | Common:2; Rare:28 | ||||
| chr7:65982132-65982342 | Common:3; Rare:70; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114776-66114971 | Common:1; Rare:90 | ||||
| chr7:66115169-66115368 | Common:1; Rare:44 | ||||
| chr7:66628676-66629011 | Common:2; Rare:122; Clinvar:6 | ||||
| chr7:66682028-66682192 | Common:6; Rare:77 | ||||
| chr7:66921133-66921478 | Common:1; Rare:106 | ||||
| chr7:66996557-66996872 | Common:2; Rare:73 | ||||
| chr7:71131449-71131721 | Common:5; Rare:93 | ||||
| chr7:72828175-72828482 | Rare:77 |